Clinical Researcher

Spirair, a venture capital-backed medical device company, was co-founded by two Stanford Biodesign and Innovation fellows with a shared interest in optimizing outcomes and patient experience through innovation solutions. With a passion for developing elegant technologies that evolve care and enhance accessibility and effectiveness, the Spirair team is partnering with leading ENT advisors and industry veterans to offer treatment options that are both massively impactful and minimally invasive.

We are looking for a Clinical Research Associate based out of the Southern, Mid-Southern, or Western US who is within one hour of a major airport. (Ideal locations would be Texas or Chicago, IL.) This is a fully remote role.

The Clinical Research Associate (CRA) will perform Spirair sponsored pre- and post-market clinical studies.  Support Clinical department in organizing and overseeing clinical studies, supervising study sites, collection, and authentication of study...

FEFA LLC is seeking a highly experienced and detail-oriented Clinical Research Quality Manager to join our team. The ideal candidate will have a strong background in overseeing clinical trials, performing quality visits, and creating Standard Operating Procedures (SOPs). This role is critical in ensuring the highest standards of quality and compliance in our clinical research activities.

Responsibilities:

• Oversee the planning, execution, and monitoring of clinical trials to ensure compliance with regulatory requirements and Good Clinical Practice (GCP) guidelines.
• Conduct quality visits to clinical trial sites to assess compliance with study protocols, SOPs, and regulatory requirements.
• Develop, review, and implement SOPs to standardize clinical research processes and ensure consistency and quality.
• Collaborate with cross-functional teams, including clinical operations, regulatory affairs, and data management, to ensure...

Clinical Research Coordinator (CRC)

Lynx Therapeutics is looking for a dedicated and knowledgeable Clinical Research Coordinator to oversee and manage clinical trials and research studies. The successful candidate will be responsible for coordinating all aspects of clinical research studies, from planning through execution, ensuring compliance with regulatory requirements, and maintaining the highest standards of quality in research practice.

Key Responsibilities:

• Plan, implement, and manage clinical trial procedures in accordance with study protocols and regulatory guidelines.
• Recruit, screen, and enroll study participants while ensuring informed consent processes are followed.
• Coordinate and schedule study visits, including participant follow-ups and data collection.
• Collaborate with healthcare professionals and research staff to facilitate smooth study operations.
• Ensure compliance with...

SAGA is seeking a talented and highly motivated Director of Clinical Research with a strong interest in advancing our mission to revolutionize cancer diagnostics through the use of liquid biopsies.

 You will be a key member of the SAGA clinical development team, an international multi-disciplinary team, where you will be responsible for providing technical and genomic expertise to key clinical studies and biopharma projects.  The trials and clinical studies may be either sponsored by SAGA or conducted in collaboration with academic, or commercial partners.  We are growing our clinical development team and engaging with world leading KOLs and so this a unique opportunity to build the clinical research, reporting to the VP of Clinical Development.

 This is an exciting opportunity to join a rapidly scaling cancer genomics startup with excellent momentum, international attention, and strong customer traction – where every role is...

About OrganOx:

OrganOx is an innovative, fast-paced, global medical device company with a mission to save lives by making every donated organ count. We are a commercial stage organ technology company, spun out of the University of Oxford in 2008, committed to improving transplantation outcomes throughout the world. The company’s first product, the OrganOx metra® normothermic machine perfusion (NMP) system for liver transplantation, has been used to support more than 4,000 liver transplant operations globally, optimizing the use of donated organs by enabling assessment of the quality of livers as well as longer preservation durations.  As part of our ongoing expansion, we seek a Clinical Training Manager to join our team.

This is an onsite, full time in-office position in Madison NJ.

Position Summary          

The Clinical Research Engineer is...

Our mission at Oura is to empower every person to own their inner potential. Our award-winning products help our global community gain a deeper knowledge of their readiness, activity, and sleep quality by using their Oura Ring and its connected app. We've helped 2.5 million people understand and improve their health by providing daily insights and practical steps to inspire healthy lifestyles.

Empowering the world starts with living our values and empowering our team. As a quickly growing company focused on helping people live healthier and happier lives, we ensure that our team members have what they need to do their best work — both in and out of the office. 

We are seeking an experienced consultant with deep expertise in the clinical research space to help shape ŌURA’s strategic direction and operational readiness for entering clinical trials and expanding into key healthcare research opportunities. This role will be pivotal in conducting market analysis,...

About CRIO: 

CRIO (Clinical Research IO) is a health tech company helping pharma, biotech, research sites, and academic research centers streamline regulatory workflows with one system and a single source of clinical data capture. Our modules allow sites to capture data electronically in real-time, providing data managers and monitors with enhanced transparency, and enabling remote monitoring by sponsors and CROs.

CRIO’s eSource and CTMS system is a leading, modern, enterprise platform built for clinical research sites. Since CRIO’s launch in 2016, CRIO has established the leading brand position in eSource and has won close to 50% of the emerging class of enterprise-grade site networks, many of whom are backed by institutional investors such as VC, PE and corporations. CRIO has achieved the attached metrics, all with little to no serious outbound sales or marketing.

In 2022, CRIO released its Reviewer product, a separate application that allows third...

Job Title: Clinical Research Coordinator (CRC)

Location: Bay Area, California

Employment Type: Full-Time, Permanent

Job Description

Stirling Q&R is seeking a dedicated and detail-oriented Clinical Research Coordinator on behalf of our confidential client. This role is based in the Bay Area and offers an exciting opportunity to manage and coordinate clinical research studies. The successful candidate will ensure compliance with regulatory standards while maintaining high-quality data collection and management.

Responsibilities

• Act as the primary contact for research participants, sponsors, and regulatory agencies.
• Screen, recruit, and obtain consent from study participants; review medical records and conduct interviews as needed.
• Schedule participant appointments and provide reminders or other necessary communications.
• Prepare and maintain...

Associate Director/Director of Clinical Research

SAGA Diagnostics is a personalized cancer diagnostics and disease monitoring company focused on molecular genetic analysis of circulating tumor DNA (ctDNA). The company’s mission is to improve precision cancer medicine, provide more accurate treatment monitoring, and improve patient survival using minimally invasive liquid biopsy cancer testing services. SAGA’s proprietary tests can help patients, oncologists, and drug developers detect actionable mutations, stratify patient groups, and monitor treatment response, residual disease, and disease recurrence at unprecedented sensitivity and scale.

SAGA is seeking a talented and highly motivated Associate Director of Clinical Research with a strong interest in advancing our mission to revolutionize cancer diagnostics through the use of liquid biopsies.

You will be a key member of the SAGA clinical development team, an international multi-disciplinary...

Northwest Clinical Trials is seeking a motivated and detail-oriented Clinical Research Coordinator to join our team. As a leading research organization in the pharmaceutical research industry, we are dedicated to improving patient care through clinical trials. In this role, you will have the opportunity to work on groundbreaking research projects and contribute to medical advancements. If you have a strong passion for healthcare, attention to detail, and excellent organizational skills, we want to hear from you!

As a Clinical Research Coordinator, you will be responsible for managing all aspects of clinical trials, from planning to execution. You will work closely with physicians, nurses, patients, and other research staff to ensure the smooth operation of trials and the collection of accurate data. Your exceptional communication skills will be essential as you will act as the point of contact for study participants, providing them with detailed information about the trials...

Company Overview: AL Solutions is partnered with a groing Biotech. With a focus on quality, innovation, and patient safety, our client is committed to driving excellence in clinical research.

Position Summary: We are currently seeking a dedicated and experienced Clinical Research Associate II (CRA II) to join our team. As a CRA II, you will be responsible for overseeing and monitoring clinical trials at various investigational sites in accordance with study protocols, Good Clinical Practice (GCP), and applicable regulatory requirements.

Responsibilities:

• Conduct site initiation, interim monitoring, and close-out visits to ensure protocol compliance and high-quality data collection.
• Perform source document verification, query resolution, and data review at study sites.
• Ensure accurate and timely completion of monitoring reports, study documentation, and regulatory filings.
• Develop...

Company:

CRIO (Clinical Research IO) is a health tech company helping pharma, biotech, research sites, and academic research centers streamline regulatory workflows with one system and a single source of clinical data capture. Our modules allow sites to capture data electronically in real-time, providing data managers and monitors with enhanced transparency, and enabling remote monitoring by sponsors and CROs.

CRIO’s eSource and CTMS system is a leading, modern, enterprise platform built for clinical research sites. Since CRIO’s launch in 2016, CRIO has established the leading brand position in eSource and has won close to 50% of the emerging class of enterprise-grade site networks, many of whom are backed by institutional investors such as VC, PE and corporations. CRIO has achieved the attached metrics, all with little to no serious outbound sales or marketing.

In 2022, CRIO released its Reviewer product, a separate application that allows third parties to...

Why work for CVRx?

CVRx pioneers' unique therapies that harness and harmonize the body’s natural systems, benefiting society and making CVRx a universal role model in healthcare. We value our commitments to others and continue to overcome challenges through determination, collaboration and purpose. If our culture and values speak to you, and if you have a passion for cutting-edge medical technologies, join our team and our mission to help others live better lives.

A day in the life:

The Clinical Research Associate Intern plays a pivotal role in driving the success of research studies by fostering strong connections with study sites and field staff. From preparing essential study materials to ensuring seamless patient reimbursements, and managing clinical payments, every task contributes to the smooth operation of the study. Additionally, actively assists Clinical Centers with IRB submissions and regulatory document...

Title:  Senior Clinical Research Associate

Location: US Remote

Position: Permanent/Full-time (40 hours/week 8.30am-530pm EST)

About Petlab Co

PetLab Co. is the world’s fastest-growing pet supplement business. Launching in 2018, we successfully achieved a 9-figure revenue in 2022 without any external funding. We have a loyal community of loving pet parents and over 1.5 million happy dogs whose lives have been positively impacted by our innovative products. Our team is vibrant, fast-moving, and customer-driven where high-performers are valued and rewarded. And it is the ideal place for an ambitious, hardworking, animal lover who wants to progress their career rapidly.

A Day In The Life…
We move and think fast so it’s important that you are able to thrive in a fast-paced environment and are happy to roll up your sleeves to do whatever it...

A multi-year Clinical Research Coordinator (CRC) position is available at our research site in Plano, TX with an initial focus on an active pulmonary study from a major pharmaceutical sponsor. Working independently under the Research Program Manager, the CRC will be responsible for carrying out clinical research studies, including but not limited to participant recruitment and enrollment, scheduling study visits, carrying out study procedures, data collection and transfer to data repositories, and maintaining study records. The CRC must be able to work in a medical clinic setting supporting the principal investigator (PI) with protocol requirements, display a high degree of initiative, and have excellent interpersonal, organizational, and time management skills.

The company is hiring full-time and part-time positions.

Interested candidates should send a current resume and introductory cover letter to s.mcauley@empowerclinics.com

May perform some or all the...

Are you a driven and detail-oriented individual with a passion for clinical research? Look no further! EPW Curesearch LLC is seeking a Clinical Research Coordinator (CRC) to join our dedicated team in Los Angeles County, CA

In this multi-year position, you will have the opportunity to work on an active pulmonary study conducted by a major pharmaceutical sponsor. As a CRC, you will be responsible for various aspects of clinical research including participant recruitment and enrollment, scheduling study visits, carrying out study procedures, data collection and transfer to data repositories, and maintaining study records. You will work closely with the Research Program Manager and support the principal investigator (PI) in meeting protocol requirements.

We are looking for someone who can thrive in a medical clinic setting, exhibit a high degree of initiative, and possess excellent interpersonal, organizational, and time management skills.

We are currently hiring for...

Global Life Science Hub is closely partnered with an incredibly specialist CRO in the Oncology space, which has a team of 400 dedicated professionals spread across various locations worldwide, and is highly selective in its partnerships. They only collaborate with the world's most boutique, small, and niche Biotech and Pharma companies, aiming to together develop life-changing therapies that can positively impact patients' lives.

In line with their expansion plans, they have recently launched new operations on the East Coast of the United States and acquired a niche CRO. These strategic moves further solidify their commitment to growth and development in the US market over the next 24 months.

As a result of their recent success, there is an exciting opportunity to join as an experienced Clinical Research Associate. This role requires someone who possesses the necessary skills and experience in clinical research and has high-reaching career aspirations....

About CRIO: 

CRIO (Clinical Research IO) is a health tech company helping pharma, biotech, research sites, and academic research centers streamline regulatory workflows with one system and a single source of clinical data capture. Our modules allow sites to capture data electronically in real-time, providing data managers and monitors with enhanced transparency, and enabling remote monitoring by sponsors and CROs.

CRIO’s eSource and CTMS system is a leading, modern, enterprise platform built for clinical research sites. Since CRIO’s launch in 2016, CRIO has established the leading brand position in eSource and has won close to 50% of the emerging class of enterprise-grade site networks, many of whom are backed by institutional investors such as VC, PE and corporations. CRIO has achieved the attached metrics, all with little to no serious outbound sales or marketing.

In 2022, CRIO released its Reviewer product, a separate application that allows third...

Atlantic Research Group (ARG), a premier Contract Research Organization (CRO) known for its dedication to advancing clinical trials in oncology, immunology, and neurology, is seeking an entry-level Clinical Research Specialist. This cross-functional role is pivotal in supporting operational activities across multiple departments, including Clinical Operations, Data Management, Drug Safety, and Project Management.

Are you ready to start your career in clinical research? Do you have a knack for organization, a sharp eye for detail, and the drive to learn about new therapeutic areas and regulations? If you are passionate about contributing to groundbreaking clinical research, we have the ideal opportunity for you.

Key Responsibilities:

• Assist in the execution of operational tasks across various departments in line with project plans and SOPs.
• Review and update data in ARG’s Clinical Management System, Electronic Data Capture, and other...

Atlantic Research Group (ARG), a distinguished Contract Research Organization (CRO) specializing in oncology, immunology, and neurology clinical trials, is seeking an experienced Clinical Research Associate (CRA) with a proven track record in monitoring clinical trials. Our focus is on helping innovators bring new therapies to market, particularly in the therapeutic areas of oncology, immunology, and neurology.

Do you have experience in clinical trial monitoring and a deep commitment to ensuring the safety and efficacy of new medical treatments? Are you ready to work in a dynamic, traveling role that places you at the forefront of medical research? If you excel in building collaborative relationships and have a keen eye for detail, consider joining our mission.

Key Responsibilities:

• Perform and coordinate all aspects of the clinical monitoring process, ensuring compliance with GCPs and ARG's global SOPs.
• Develop and maintain...

The Kestra team has over 400 years of experience in the external and internal cardiac medical device markets. The company was founded in 2014 by industry leaders inspired by the opportunity to unite modern wearable technologies with proven device therapies. Kestra’s solutions combine high quality and technical performance with a wearable design that provides the greatest regard for patient comfort and dignity. Innovating versatile new ways to deliver care, Kestra is helping patients and their care teams harmoniously monitor, manage, and protect life.

In this role, you will have responsibility for managing all aspects of Kestra sponsored clinical trials for the generation of clinical evidence for the ASSURE wearable cardioverter defibrillator (WCD) system and other portfolio products.

Requirements

ESSENTIAL DUTIES:

• Manage all aspects of the ASSURE Patient Registry study including clinical data management, analysis,...

The Senior Clinical Research Coordinator (CRC) is a specialized research professional working with and under the direction of the clinical Principal Investigator (PI). While the Principal Investigator is primarily responsible for the overall design, conduct, and management of the clinical trial, the CRC supports, facilitates and coordinates the daily clinical trial activities and plays a critical role in the conduct of the study. By performing these duties, the CRC works with the PI and internal teams to support and provide guidance on the administration of the compliance, financial, personnel and other related aspects of the clinical study.

The Senior Clinical Research Coordinator will coordinate all research-related activities, including the initial set-up of the study, study participant recruitment and retention, delivery of the intervention, data collection, entry, and quality control activities, protocol compliance and patient safety. He/She will also work on monitoring...

The Alliance for Clinical Trials in Oncology Foundation (Foundation) is a foundation created to enhance and expand the ability of the Alliance for Clinical Trials in Oncology (Alliance) to conduct cancer clinical research and address important treatment questions through large-scale clinical trials. Through efforts of the Foundation in support of the Alliance, clinical trials and laboratory research are conducted to discover new or improved ways to prevent, treat, and cure many types of cancer, including leukemia and lymphoma, and cancers of the breast, prostate, lung, and gastrointestinal (GI) tract, and help educate the medical community on methods of cancer diagnosis, treatment, and prevention.

The Alliance for Clinical Trials in Oncology Foundation is looking for a Clinical Trial Research Nurse who is excited to provide clinical expertise and oversight to clinical trials from the initial study design through the final study close-out. We are an organization of passionate,...

Company Description

LVIS Corporation is on a mission to revolutionize the entire continuum of neurological care by developing AI driven software tools to help physicians accelerate patient throughput and improve patient diagnostic and treatment outcomes. We have an international team with our headquarters located in Palo Alto, California, USA, and we have an office in Gangnam, Seoul, South Korea. We are looking for talented individuals to join us in our mission to transform the neurology health care industry.

Key responsibilities:

• You’ll be responsible for the collection, validation, and organization of LVIS’ clinical data in compliance with regulatory requirements.
• Collaborating with other team members to ensure accuracy and timely data delivery.
• Clinical database management, ensuring data integrity, consistency, and compliance.
• Preparation and management of clinical trial-related...

ATEC Spine has an exciting opportunity for a Senior Manager of Clinical Research & Strategy as a member of the Scientific Affairs team located in Carlsbad, California. ATEC’s Scientific Affairs team is responsible for regulatory, testing, and research activities supporting the company’s initiatives. The Clinical Research function, as a sub-function of Scientific Affairs, includes planning, coordinating, and overseeing the successful execution of preclinical and clinical research studies and large-scale data collection efforts in partnership with our surgical practice partners. Specifically, the Senior Manager of Clinical Research & Strategy position is responsible for defining the strategic direction, resourcing, and managing the execution of the company’s clinical evidence strategy, including site-initiated and sponsored protocol-driven research studies and registry data collection and utility.

SUMMARY

From evidence generation...

An ATEC Clinical Research Manager (CRM) supports the company’s Clinical Research initiatives by managing the clinical research operations and successful execution of clinical studies and data collection efforts in partnership with our clinical practice partners. Specifically, the position is responsible for the management of research activities spanning from development of study documents, to site start-up and recruitment of study participants, collection and compilation of study data, assists with site data management and analysis oversight of site monitoring and reporting of site performance and adherence to protocols following Good Clinical Practices, and input toward the reporting of study results. In a team supervisory capacity, the CRM develops project budgets and operating procedures and documents, supervises in-house and field-based monitoring staff, and ensures that project milestones are met while managing adherence to approved budgets. The role collaborates closely...

The Clinical Research Monitor will work under the Executive Director of Clinical Trial Operations and the Associate Director of Clinical Trial Operations to oversee activity at Alliance for Clinical Trials in Oncology sites participating in Alliance Foundation Trials (AFT) clinical trials. This position is responsible for completing clinical monitoring activities at participating sites. This includes Source Data Validation (SDV) of clinical study data entered on the Case Report Forms (CRF) in the Electronic Data Capture (EDC) system, review and reconciliation of the Investigational Site File (ISF) with the Electronic Trial Master File (eTMF), ensure proper documentation of Investigational Product (IP), and ensure overall adherence to protocol procedures. The Clinical Research Monitor works in partnership with the AFT Project Manager and individual study teams to complete all site monitoring activities across assigned AFT projects and ensures all participating sites are compliant...